R&D Systems Inc. Tocris Bioscience Boston Biochem

Sar-[D-Phe8]-des-Arg9-Bradykinin

Cat. No. 3230

Sar-[D-Phe8]-des-Arg9-Bradykinin Sar-Arg-Pro-Pro-Gly-Phe-Ser-Pro-D-Phe

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Biological Activity

Potent and selective bradykinin B1 receptor agonist (EC50 = 9.02 nM in rabbit aorta) that is resistant to aminopeptidase, kininase I and II (ACE) and neutral endopeptidase cleavage. Exhibits hypotensive and angiogenic activity in vivo.

Technical Data

M.Wt:
975.11
Formula:
C47H66N12O11
Sequence:
XRPPGFSPF

(Modifications: X = Sar, Phe-9 = D-Phe)

Solubility:
Soluble to 2 mg/ml in 30% acetonitrile / water
Storage:
Desiccate at -20°C
CAS No:
126959-88-4

The technical data provided above is for guidance only.
For batch specific data refer to the Certificate of Analysis.

Certificate of Analysis / Safety Data Sheet

Certificate of Analysis: View current batch
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Safety Data Sheet: View Safety Data Sheet

References

Drapeau et al (1991) Hypotensive effects of Lys-des-Arg9-Bradykinin and metabolically protected agonists of B1 receptors for kinins. J.Pharmacol.Exp.Ther. 259 997. PMID: 1662280.

Drapeau et al (1993) Development and in vivo evaluation of metabolically resistant antagonists of B1 receptors for kinins. J.Pharmacol.Exp.Ther. 266 192. PMID: 8392550.

Leeb-Lundberg et al (2005) International union of pharmacology. XLV. Classification of the kinin receptor family: from molecular mechanisms to pathophysiological consequences. Pharmacol.Rev. 57 27. PMID: 15734727.

If you know of a relevant citation for this product please let us know.

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Keywords: Sar-[D-Phe8]-des-Arg9-Bradykinin, supplier, Potent, selective, B1, agonists, Receptors, Bradykinin

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